Enhanced activity and durability of novel activated carbon-supported PdSn heat-treated cathode catalyst for polymer electrolyte fuel cells
Novel carbon-supported PdSn electrocatalysts for ORR in PEFCs were synthesized by NaBH4 reduction method with and without carbon activation pre-treatment (i.e., Sn sensitization and Pd activation) followed by heat treatment at 300°C in a H2/N2 mixture and compared with Pd. The catalysts were charact...
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Veröffentlicht in: | Electrochimica acta 2016-02, Vol.192, p.268-282 |
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Sprache: | eng |
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Zusammenfassung: | Novel carbon-supported PdSn electrocatalysts for ORR in PEFCs were synthesized by NaBH4 reduction method with and without carbon activation pre-treatment (i.e., Sn sensitization and Pd activation) followed by heat treatment at 300°C in a H2/N2 mixture and compared with Pd. The catalysts were characterized by EDX, XRD, TEM/SAED and XPS. The electrocatalytic activity for ORR was tested in acid medium using cyclic voltammetry, rotating disc electrode and chronoamperometry. For the first time, these catalysts were tested in a single H2/O2 PEM fuel cell. Rotating disc electrode studies indicated that the new catalysts PdSn-3H and PdSn-2H exhibited, respectively, 10 and 4 times higher ORR activity than Pd catalyst, as well as higher methanol and ethanol tolerance. ORR proceeded through a 4-electron reduction pathway on both heat-treated catalysts. The new catalysts also exhibited improved electrochemical durability under potential cycling (600 cycles from −0.2 to 1.0V) and constant potential (-0.55V, 40h). The observed high activity and durability of these catalysts may be attributed to: i) their specific alloying composition at their surface; ii) the graphitization degree of the carbon support and/or, iii) the presence of intermetallic compounds. H2/O2 single fuel cell based on PdSn-2H cathode operating at 60°C exhibited the highest ORR mass activity (1.36AmgPd−1at 0.6V) among the previous results obtained in the literature on PdSnPt, Pd-based and Pd catalysts. |
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ISSN: | 0013-4686 1873-3859 |
DOI: | 10.1016/j.electacta.2016.01.177 |